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Anoxia Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K232831Quiver Aspiration PumpFebruary 22, 2024
K231179Slinky CatheterDecember 1, 2023